Variant report

Variant rs6424934
Chromosome Location chr1:184188537-184188538
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:184162600-184191400 Weak transcription Right Ventricle heart
2 chr1:184179400-184191800 Weak transcription Fetal Kidney kidney
3 chr1:184179600-184191600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
4 chr1:184180200-184194400 Weak transcription Fetal Brain Male brain
5 chr1:184182400-184189400 Weak transcription Spleen Spleen
6 chr1:184182400-184193400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
7 chr1:184182400-184195400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
8 chr1:184182600-184192000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
9 chr1:184183400-184191400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
10 chr1:184186800-184188800 Enhancers Cortex derived primary cultured neurospheres brain
11 chr1:184187600-184188600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr1:184187600-184189000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr1:184187600-184189000 Enhancers NHDF-Ad bronchial
14 chr1:184188000-184188600 Enhancers Osteobl bone
15 chr1:184188200-184191600 Weak transcription Fetal Brain Female brain
16 chr1:184188200-184191800 Weak transcription Brain Substantia Nigra brain
17 chr1:184188200-184192000 Weak transcription Brain Anterior Caudate brain

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